Duration & Type: 12 months Contract with a major pharmaceutical industry client
Location: San Dieogo, California
Responsibilities:
- The main responsibility for the Synthesis and Production Microbiology Supervisor is to lead and oversee all production activities associated with oligo synthesis and production microbiology in a multi-product cGMP facility.
- The Supervisor will gather and analyze Key Performance Indicator (KPI) data related to manufacturing to identify opportunities for continuous improvement.
- The Supervisor must collaborate with cross-functional partners, such as Supply Chain, Manufacturing Sciences, Manufacturing Technical Support, Quality Assurance, Quality Control, Validation and Facilities to accomplish organizational objectives (e.g., meeting commercial demand, new process transfers, new manufacturing area commissioning and validation).
Required:
- Education: Bachelor’s degree or Master’s degree in (Bio)chemistry, Chemical Engineering, Microbiology, Biology or related field.
- 6+ years of related GMP experience in a laboratory or commercial manufacturing setting with a Bachelor’s degree or 4+ years of related GMP experience in a laboratory or commercial manufacturing setting with a Master’s degree
- 2+ years of supervisory or team leadership experience
For consideration, please send resume to [email protected]
